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#618890 - NEURODEVELOPMENTAL DISORDER AND STRUCTURAL BRAIN ANOMALIES WITH OR WITHOUT SEIZURES AND SPASTICITY; NEDBASS
Cytogenetic locations: 27848944
Gene summaries Genetic tests Medical literature
#618548 - MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 4; MCAHS4
Cytogenetic locations: 31148362
#618348 - GALLOWAY-MOWAT SYNDROME 7; GAMOS7
Cytogenetic locations: 28280135
#618221 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 66; MRT66
Cytogenetic locations: 28097321
#617913 - NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES; NEDMCR
Cytogenetic locations: 27878435
#617822 - ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS
Cytogenetic locations: 611574
#617020 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 38; DEE38
Cytogenetic locations: 27270415
#616900 - HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3; IHPRF3
Cytogenetic locations: 27040692
*616899 - TBC1 DOMAIN-CONTAINING KINASE; TBCK
Cytogenetic locations: 24576458
*616082 - CHROMOSOME 12 OPEN READING FRAME 4; C12ORF4
*614387 - ZINC FINGER PROTEIN 526; ZNF526
Cytogenetic locations: 21937992
*612324 - COILED-COIL DOMAIN-CONTAINING PROTEIN 34; CCDC34
Cytogenetic locations: 16554811
#612100 - AUTISM, SUSCEPTIBILITY TO, 15; AUTS15
Cytogenetic locations: 611050
*611565 - BRIDGE-LIKE LIPID TRANSFER PROTEIN FAMILY, MEMBER 1; BLTP1
Cytogenetic locations: 19640479
#610185 - CEREBELLAR ATAXIA, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSEQUILIBRIUM SYNDROME 2; CAMRQ2
Cytogenetic locations: Rfwd3
*607796 - PHD FINGER PROTEIN 11; PHF11
Cytogenetic locations: 12754510
*607740 - UBIQUITIN-SPECIFIC PROTEASE 32; USP32
Cytogenetic locations: 10508479
*606584 - PROTEIN-TYROSINE PHOSPHATASE, NONRECEPTOR-TYPE, 23; PTPN23
*604569 - CONTACTIN-ASSOCIATED PROTEIN-LIKE 2; CNTNAP2
Cytogenetic locations: 19896112
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